Clearance Summary
MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES received FDA 510(k) clearance under submission number K915821, sponsored by Kerma Medical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1992-05-29.
- Submission: K915821
- Applicant / Sponsor: Kerma Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4014
- Decision date: 1992-05-29
Classification & Regulation
This clearance is catalogued under FDA product code NAB and 21 CFR 878.4014, within the General, Plastic Surgery review panel as a Class I device.